Canonical Allele Identifier: CA2814387115
Gene: AKT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285352_40285353insAAA , CM000681.2:g.40285352_40285353insAAA GRCh38
NC_000019.9:g.40791259_40791260insAAA , CM000681.1:g.40791259_40791260insAAA GRCh37
NC_000019.8:g.45483099_45483100insAAA NCBI36
NG_012038.2:g.5006_5007insTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000391844.8:c.-303_-302insTTT ENSP00000375719.4:n.-303_-302insTTT
ENST00000392038.6:c.-257_-256insTTT ENSP00000375892.2:n.-257_-256insTTT
ENST00000424901.5:c.-257_-256insTTT ENSP00000399532.2:n.-257_-256insTTT
ENST00000578123.5:c.-85+95_-85+96insTTT ENSP00000462022.1:n.-85+95_-85+96insTTT
NM_001243027.2:c.-406_-405insTTT NP_001229956.1:n.-406_-405insTTT
NM_001243028.2:c.-313_-312insTTT NP_001229957.1:n.-313_-312insTTT
NM_001626.5:c.-257_-256insTTT NP_001617.1:n.-257_-256insTTT
XM_011526620.1:c.-85+95_-85+96insTTT XP_011524922.1:n.-85+95_-85+96insTTT